Abrupt Transition of Nanothermite Reactivity: The Roles of Loading Density, Microstructure and Ingredients

纳米热剂反应活性的突变:负载密度、微观结构和成分的作用

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Abstract

Nanothermites are widely applied as specific power sources for microscale initiators and pyrotechnics. Increasing the charge density enhances energy storage within a confined combustion chamber, but it also alters the reaction kinetics. To systemically explore this phenomenon, the combustion and pressurization characteristics of electrosprayed nanothermite-based hybrid energetic materials (THEMs) with different metallic oxides (Fe(2)O(3), CuO, and Bi(2)O(3)) and various energetic additives (nitrocellulose (NC), octogen (HMX), ammonium perchlorate (AP), and hexanitrohexaazaisowurtzitane (CL-20)) across various loading densities were tested. The results showed that increasing the loading density decreased the porosity of the loaded nanothermites and then rapidly decreased the convective heat transfer efficiency during the combustion propagation process. When the loading density exceeded a critical value, a dramatic decrease in the peak pressure, several orders-of-magnitude decrease in the pressurization rate, and an order-of-magnitude increase in the combustion duration occurred. Due to the dual effects of the porous microstructure on heat and mass transfer, the critical density of both the electrosprayed Al/CuO/NC/CL-20 composites and their physically mixed counterparts is between 37.9 and 43.9% theoretical maximum density (TMD). Because of the different synergistic catalytic effects, the fast reactivity at the high-loading-density maintaining capacity of the applied additives was AP > HMX ≈ CL-20 > NC. Owing to their intrinsic properties of low ignition temperature and high gas yield, the Bi(2)O(3)-THEMs could maintain high-speed reactivity even at 59.7% TMD. These results provide valuable insights into the rational design and tailoring of the reactivity of nanothermites for specific applications.

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